PROGESTERONE
- Product NDC
- 69452-234
- 11-digit product format
- 694520234
- Labeler code
- 69452
- Product ID
- 69452-234_3e777dbd-754b-9d2e-e063-6294a90a42a6
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- PROGESTERONE
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Bionpharma Inc.
- Application
- ANDA200900
- Marketing category
- ANDA
- Marketing start
- 2018-11-28
- Substance
- PROGESTERONE
- Active strength
- 200 mg/1
- Pharmacologic classes
- Progesterone [CS], Progesterone [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- PROGESTERONE
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| PROGESTERONE | 200 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 4G7DS2Q64Y |
| Rxcui | 260243, 312641 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 69452-234-20 | PROGESTERONE | 100 in 1 BOTTLE | CAPSULE | 100 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 69452-234 | PROGESTERONE CAPSULE [BIONPHARMA INC.] | 3 | Current NDC, Legacy NDC, 1 package rows | 20250308_41b3c3a7-5fb8-4451-a96c-2bd02613c021.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 69452-234-20 | 69452023420 | 100 CAPSULE in 1 BOTTLE (69452-234-20) | 100 capsule | 2018-11-28 | 0000-00-00 | No | No | Current |